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The transgenic construct contains a full length human dystrophin gene modified by the deletion of the H2 domain and deletion of spectrin-like repeat 4 through repeat 19 and the C-terminus to generate a micro-dystrophin cDNA (DH2-R19) under the control of the human skeletal alpha 1 actin (ACTA1) promoter. (J:146281)
Basic Information
Allele
Strain of Origin
Allele Type
Mutation
Inheritance
Gene Expression
Related Disease
Reference
Phenotypes
Legend：
hm: homozygous
ht: heterozygous
cn: conditional genotype
cx: complex: > 1 genome feature
tg: involves transgenes
ot: other: hemizygous, indeterminate,...
(F): Female
(M): Male
phenotype observed
N: normal phenotype
(#): related diseases count
Phenotypes：
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| Phenotypes |
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References Literature
Title
PMID
Journal
Year
IF
